Aušra Matulevičienė

498 total citations
24 papers, 348 citations indexed

About

Aušra Matulevičienė is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Aušra Matulevičienė has authored 24 papers receiving a total of 348 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 12 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Aušra Matulevičienė's work include Genomic variations and chromosomal abnormalities (6 papers), Cleft Lip and Palate Research (6 papers) and Craniofacial Disorders and Treatments (4 papers). Aušra Matulevičienė is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Cleft Lip and Palate Research (6 papers) and Craniofacial Disorders and Treatments (4 papers). Aušra Matulevičienė collaborates with scholars based in Lithuania, Latvia and Estonia. Aušra Matulevičienė's co-authors include Vaidutis Kučinskas, Laima Ambrozaitytė, Algirdas Utkus, Mare Saag, Triin Jagomägi, Andres Metspalu, Tiit Nikopensius, Thomy de Ravel, Ilze Akota and Baiba Lāce and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Medicine.

In The Last Decade

Aušra Matulevičienė

23 papers receiving 344 citations

Peers

Aušra Matulevičienė
Teresa Neuhann Germany
Muriel Holder France
Florencia Giliberto Argentina
Sophie Scheidecker France
Filomena Tiziana Papa Italy
Anneke T. Vulto‐van Silfhout Netherlands
Jenina Capasso United States
Sophie Walraedt Belgium
G Morin France
Siren Berland Norway
Teresa Neuhann Germany
Aušra Matulevičienė
Citations per year, relative to Aušra Matulevičienė Aušra Matulevičienė (= 1×) peers Teresa Neuhann

Countries citing papers authored by Aušra Matulevičienė

Since Specialization
Citations

This map shows the geographic impact of Aušra Matulevičienė's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Aušra Matulevičienė with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aušra Matulevičienė more than expected).

Fields of papers citing papers by Aušra Matulevičienė

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aušra Matulevičienė. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Aušra Matulevičienė. The network helps show where Aušra Matulevičienė may publish in the future.

Co-authorship network of co-authors of Aušra Matulevičienė

This figure shows the co-authorship network connecting the top 25 collaborators of Aušra Matulevičienė. A scholar is included among the top collaborators of Aušra Matulevičienė based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Aušra Matulevičienė. Aušra Matulevičienė is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Lesinskienė, Sigita, et al.. (2024). Neuropsychiatric Aspects of Sotos Syndrome: Explorative Review Building Multidisciplinary Bridges in Clinical Practice. Journal of Clinical Medicine. 13(8). 2204–2204. 3 indexed citations
2.
Kazlauskas, Evaldas, Giedrė Smailytė, Vaidutis Kučinskas, et al.. (2023). Psychological distress 35 years after the Chornobyl accident in the Lithuanian clean-up workers. Global Health Action. 16(1). 2233843–2233843.
3.
Matulevičienė, Aušra, et al.. (2023). Consensus recommendations on chewing, swallowing and gastrointestinal problems in Phelan-McDermid syndrome. European Journal of Medical Genetics. 66(6). 104763–104763. 10 indexed citations
4.
Strumila, Robertas, et al.. (2021). Significant Association Between Huntingtin Gene Mutation and Prevalence of Hopelessness, Depression and Anxiety Symptoms. SHILAP Revista de lepidopterología. 28(1). 77–85. 2 indexed citations
5.
Cimbalistienė, Loreta, et al.. (2021). A novel variant in the PDE4D gene is the cause of Acrodysostosis type 2 in a Lithuanian patient: a case report. BMC Endocrine Disorders. 21(1). 71–71. 1 indexed citations
6.
Lesinskienė, Sigita, et al.. (2020). Juvenile Huntington’s disease: two case reports and a review of the literature. Journal of Medical Case Reports. 14(1). 173–173. 7 indexed citations
7.
Meyer, Robert, Laima Ambrozaitytė, Aušra Matulevičienė, et al.. (2020). HMGA2 Variants in Silver-Russell Syndrome: Homozygous and Heterozygous Occurrence. The Journal of Clinical Endocrinology & Metabolism. 105(7). 2401–2407. 13 indexed citations
8.
Matulevičienė, Aušra, et al.. (2017). Opposite chromosome constitutions due to a familial translocation t(1;21)(q43;q22) in 2 cousins with development delay and congenital anomalies. Medicine. 96(16). e6521–e6521. 5 indexed citations
9.
Jakaitienė, Audronė, Eglė Preikšaitienė, Birutė Burnytė, et al.. (2016). The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population. BMC Genetics. 17(1). 45–45. 18 indexed citations
10.
Inashkina, Inna, Eriks Jankevics, Ieva Mičule, et al.. (2016). Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies. BMC Musculoskeletal Disorders. 17(1). 200–200. 8 indexed citations
11.
Meyer, Robert, G. Fekete, Stephanie Spranger, et al.. (2016). NSD1 duplication in Silver–Russell syndrome (SRS): molecular karyotyping in patients with SRS features. Clinical Genetics. 91(1). 73–78. 20 indexed citations
12.
Matulevičienė, Aušra, et al.. (2015). Frame shift mutations of the ZMPSTE24 gene in two siblings with restrictive dermopathy. Clinical Dysmorphology. 25(1). 7–11. 5 indexed citations
13.
Ambrozaitytė, Laima, Ilze Akota, Astrīda Krūmiņa, et al.. (2014). Association of BMP4 polymorphisms with non-syndromic cleft lip with or without cleft palate and isolated cleft palate in Latvian and Lithuanian populations.. PubMed. 16(3). 94–101. 10 indexed citations
14.
Matulevičienė, Aušra, et al.. (2013). Familial Distal Monosomy 5p15.3-pter With Trisomy 12q24.2-qter Resulting in Neurodevelopmental Delay and Dysmorphic Features. Journal of Child Neurology. 29(3). 399–405. 1 indexed citations
15.
Kasnauskienė, Jūratė, Eglė Preikšaitienė, Aušra Matulevičienė, et al.. (2012). A single gene deletion on 4q28.3: PCDH18 – A new candidate gene for intellectual disability?. European Journal of Medical Genetics. 55(4). 274–277. 15 indexed citations
16.
Nikopensius, Tiit, Laima Ambrozaitytė, Triin Jagomägi, et al.. (2011). Variation in FGF1, FOXE1, and TIMP2genes is associated with nonsyndromic cleft lip with or without cleft palate. Birth Defects Research Part A Clinical and Molecular Teratology. 91(4). 218–225. 38 indexed citations
17.
Coppieters, Frauke, Ingele Casteels, Françoise Meire, et al.. (2010). Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes. Human Mutation. 31(10). E1709–E1766. 110 indexed citations
18.
Nikopensius, Tiit, Triin Jagomägi, Kaarel Krjutškov, et al.. (2010). Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate. Birth Defects Research Part A Clinical and Molecular Teratology. 88(9). 748–756. 37 indexed citations
19.
Nikopensius, Tiit, Laima Ambrozaitytė, Kerstin U. Ludwig, et al.. (2009). Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients. American Journal of Medical Genetics Part A. 149A(11). 2551–2553. 30 indexed citations
20.
Matulevičienė, Aušra, et al.. (2007). Orofacial clefts with associated anomalies in Lithuania. Acta medica Lituanica. 14(1). 17–23. 2 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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